A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601049



Internal ID20974120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164267636..164270704hg38UCSC Ensembl
chr6:164688669..164691737hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383069
hg193069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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